Lund Crick, Schneider Marguerite, Davies Thandi, Nyatsanza Memory, Honikman Simone, Bhana Arvin, Bass Judith, Bolton Paul, Dewey Michael, Joska John, Kagee Ashraf, Myer Landon, Petersen Inge, Prince Martin, Stein Dan J, Thornicroft Graham, Tomlinson Mark, Alem Atalay, Susser Ezra
Alan J Flisher Centre for Public Mental Health, Department of Psychiatry and Mental Health, University of Cape Town, 46 Sawkins Road, Rondebosch, Cape Town, South Africa.
Trials. 2014 Nov 21;15:457. doi: 10.1186/1745-6215-15-457.
Maternal depression carries a major public health burden for mothers and their infants, yet there is a substantial treatment gap for this condition in low-resourced regions such as sub-Saharan Africa. To address this treatment gap, the strategy of "task sharing" has been proposed, involving the delivery of interventions by non-specialist health workers trained and supervised by specialists in routine healthcare delivery systems. Several psychological interventions have shown benefit in treating maternal depression, but few have been rigorously evaluated using a task sharing approach. The proposed trial will be the first randomised controlled trial (RCT) evaluating a task sharing model of delivering care for women with maternal depression in sub-Saharan Africa. The objective of this RCT is to determine the effectiveness and cost-effectiveness of a task sharing counseling intervention for maternal depression in South Africa.
METHODS/DESIGN: The study is an individual-level two-arm RCT. A total of 420 depressed pregnant women will be recruited from two ante-natal clinics in a low-income township area of Cape Town, using the Edinburgh Postnatal Depression Scale to screen for depression; 210 women will be randomly allocated to each of the intervention and control arms. The intervention group will be given six sessions of basic counseling over a period of 3 to 4 months, provided by trained community health workers (CHW)s. The control group will receive three monthly phone calls from a CHW trained to conduct phone calls but not basic counseling. The primary outcome measure is the 17-Item Hamilton Depression Rating Scale (HDRS-17). The outcome measures will be applied at the baseline assessment, and at three follow-up points: 1 month before delivery, and 3 and 12 months after delivery. The primary analysis will be by intention-to-treat and secondary analyses will be on a per protocol population. The primary outcome measure will be analyzed using linear regression adjusting for baseline symptom severity measured using the HDRS-17.
The findings of this trial can provide policy makers with evidence regarding the effectiveness and cost-effectiveness of structured psychological interventions for maternal depression delivered by appropriately trained and supervised non-specialist CHWs in sub-Saharan Africa.
Clinical Trials (ClinicalTrials.gov): NCT01977326, registered on 24/10/2013; Pan African Clinical Trials Registry (http://www.pactr.org): PACTR201403000676264, registered on 11/10/2013.
孕产妇抑郁症给母亲及其婴儿带来了重大的公共卫生负担,但在撒哈拉以南非洲等资源匮乏地区,针对这种疾病的治疗存在巨大差距。为了弥补这一治疗差距,人们提出了“任务分担”策略,即在常规医疗服务体系中,由经过专家培训和监督的非专科医护人员提供干预措施。几种心理干预措施已显示出对治疗孕产妇抑郁症有益,但很少有研究采用任务分担方法进行严格评估。拟进行的试验将是第一项随机对照试验(RCT),评估在撒哈拉以南非洲为患有孕产妇抑郁症的妇女提供护理的任务分担模式。这项RCT的目的是确定南非针对孕产妇抑郁症的任务分担咨询干预措施的有效性和成本效益。
方法/设计:该研究是一项个体水平的双臂RCT。将在开普敦一个低收入城镇地区的两家产前诊所招募总共420名抑郁的孕妇,使用爱丁堡产后抑郁量表筛查抑郁症;210名妇女将被随机分配到干预组和对照组。干预组将在3至4个月的时间内接受由经过培训的社区卫生工作者(CHW)提供的六次基本咨询。对照组将每月接到一名经过培训可进行电话沟通但不提供基本咨询的CHW打来的三次电话。主要结局指标是17项汉密尔顿抑郁评定量表(HDRS - 17)。结局指标将在基线评估时以及三个随访点应用:分娩前1个月、分娩后3个月和12个月。主要分析将采用意向性分析,次要分析将针对符合方案人群。主要结局指标将使用线性回归进行分析,并对使用HDRS - 17测量的基线症状严重程度进行调整。
该试验的结果可为政策制定者提供证据,证明在撒哈拉以南非洲由经过适当培训和监督的非专科CHW提供的针对孕产妇抑郁症的结构化心理干预措施的有效性和成本效益。
临床试验(ClinicalTrials.gov):NCT01977326,于2013年10月24日注册;泛非临床试验注册中心(http://www.pactr.org):PACTR201403000676264,于2013年10月11日注册。